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人前列腺癌中的血小板型12-脂氧合酶刺激血管生成和肿瘤生长。

Platelet-type 12-lipoxygenase in a human prostate carcinoma stimulates angiogenesis and tumor growth.

作者信息

Nie D, Hillman G G, Geddes T, Tang K, Pierson C, Grignon D J, Honn K V

机构信息

Department of Radiation Oncology, Wayne State University School of Medicine, Detroit, Michigan 48202, USA.

出版信息

Cancer Res. 1998 Sep 15;58(18):4047-51.

PMID:9751607
Abstract

Previously, we found a positive correlation between the expression of platelet-type 12-lipoxygenase (12-LOX) and the progression of human prostate adenocarcinoma (PCa; Gao et al., Urology, 46: 227-237, 1995). To determine the role of 12-LOX in PCa progression, we generated stable 12-LOX-transfected PC3 cells, which synthesize high levels of 12-LOX protein and 12(S)-hydroxyeicosatetraenoic acid metabolite. In vitro, 12-LOX-transfected PC3 cells demonstrated a proliferation rate similar to neo controls. However, following s.c. injection into athymic nude mice, 12-LOX-transfected PC3 cells formed larger tumors than did the controls. Decreased necrosis and increased vascularization were observed in the tumors from 12-LOX-transfected PC3 cells. Both endothelial cell migration and Matrigel implantation assays indicate that 12-LOX-transfected PC3 cells were more angiogenic than their neo controls. These data indicate that 12-LOX stimulates human PCa tumor growth by a novel angiogenic mechanism.

摘要

此前,我们发现血小板型12-脂氧合酶(12-LOX)的表达与人类前列腺腺癌(PCa)的进展呈正相关(Gao等人,《泌尿外科》,46: 227 - 237,1995)。为了确定12-LOX在PCa进展中的作用,我们构建了稳定转染12-LOX的PC3细胞,其能合成高水平的12-LOX蛋白和12(S)-羟基二十碳四烯酸代谢物。在体外,转染12-LOX的PC3细胞的增殖速率与新霉素对照相似。然而,皮下注射到无胸腺裸鼠体内后,转染12-LOX的PC3细胞形成的肿瘤比对照更大。在转染12-LOX的PC3细胞形成的肿瘤中观察到坏死减少和血管生成增加。内皮细胞迁移试验和基质胶植入试验均表明,转染12-LOX的PC3细胞比其新霉素对照具有更强的血管生成能力。这些数据表明,12-LOX通过一种新的血管生成机制刺激人类PCa肿瘤生长。

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